A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv965753



Internal ID18254297
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:110893419..110895696hg38UCSC Ensembl
Innerchr6:111214622..111216899hg19UCSC Ensembl
Innerchr6:111321315..111323592hg18UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg382278
hg192278
hg182278
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2420317, nssv2420319, nssv2420316, nssv2420318, nssv2420314, nssv2420321, nssv2420313, nssv2420320, nssv2420312, nssv2420315
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesAMD1
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv965753
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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